Watts Colin
Division of Cell Signaling & Immunology, College of Life Sciences, University of Dundee, Dundee, UK.
Biochim Biophys Acta. 2012 Jan;1824(1):14-21. doi: 10.1016/j.bbapap.2011.07.006. Epub 2011 Jul 18.
For a long time the lysosomal pathway was thought to be exclusively one for catabolism and recycling of material taken up by endocytosis from the external milieu or from the cytosol by autophagy. At least in the immune system it is clear now that endo/lysosomal proteolysis generates crucially important information, in particular peptides that bind class II MHC molecules to create ligands for survey by the diverse antigen receptors of the T lymphocyte system. This process of antigen processing and presentation is used to display not only foreign but also self peptides and therefore is important for 'self' tolerance as well as immunity to pathogens. Some cells, macrophages and particularly dendritic cells can load peptides on class I MHC molecules in the endosome system through the important, though still not fully characterised, pathway of cross-presentation. Here I try to provide a brief review of how this area developed focussing to some extent our own contributions to understanding the class II MHC pathway. I also mention briefly recent work of others showing that proteolysis along this pathway turns out to regulate immune signalling events in the innate immune system such as the activation of some members of the Toll-like receptor family. Finally, our recent work on the endo/lysosome targeted protease inhibitor cystatin F, suggests that auto-regulation of protease activity in some immune cells occurs. This article is part of a Special Issue entitled: Proteolysis 50 years after the discovery of lysosome.
长期以来,溶酶体途径一直被认为是专门用于分解代谢和循环利用通过内吞作用从细胞外环境摄取的物质或通过自噬从细胞质摄取的物质的途径。至少在免疫系统中,现在很清楚的是,内吞/溶酶体蛋白水解产生至关重要的信息,特别是与II类MHC分子结合以产生配体供T淋巴细胞系统的各种抗原受体检测的肽。这种抗原加工和呈递过程不仅用于展示外来肽,也用于展示自身肽,因此对于“自身”耐受性以及对病原体的免疫都很重要。一些细胞,如巨噬细胞,特别是树突状细胞,可以通过重要但仍未完全表征的交叉呈递途径,在内体系统中将肽加载到I类MHC分子上。在这里,我试图简要回顾一下这个领域是如何发展的,在一定程度上聚焦于我们自己对理解II类MHC途径的贡献。我还简要提及了其他人最近的工作,这些工作表明沿着这条途径的蛋白水解结果是调节先天性免疫系统中的免疫信号事件,如Toll样受体家族某些成员的激活。最后,我们最近关于靶向内吞/溶酶体的蛋白酶抑制剂胱抑素F的工作表明,一些免疫细胞中存在蛋白酶活性的自我调节。本文是名为:溶酶体发现50年后的蛋白水解的特刊的一部分。